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PROFOUNDCustomizable, Incision-Free Ablation Therapies
CORPORATE PRESENTATION | SEPTEMBER 2019
© 2019 PROFOUND MEDICAL CORP. | TSX: PRN | OTCQX: PRFMF
Certain statements in this presentation and oral statements made during this meeting may contain “forward-looking statements” within the meaning of applicable securities laws, including the
“safe harbour provisions” of the Securities Act (Ontario), with respect to Profound Medical Corporation (“Profound” or the “Company”). Such statements include all statements other than
statements of historical fact contained in this presentation, such as statements that relate to the Company’s current expectations and views of future events. Often, but not always, forward-
looking statements can be identified by the use of words such as “may”, “will”, “expect”, “anticipate”, “predict”, “aim”, “estimate”, “intend”, “plan”, “seek”, “believe”, “potential”, “continue”, “is/are
likely to”, “is/are projected to” or the negative of these terms, or other similar expressions, as well as future or conditional verbs such as “will”, “should”, “would”, and “could” intended to identify
forward-looking statements. These forward-looking statements include, among other things, statements relating to expectations regarding future clinical trials, expectations regarding regulatory
approvals, expectations regarding the safety and efficacy of its products, our expectations regarding commercializing our approved products (particularly the TULSA-PRO system following FDA
clearance) and our ability to generate revenues and achieve profitability; our expectations regarding the safety, efficacy and advantages of our products over our competitors and alternative
treatment options; our expectations regarding our products fulfilling unmet clinical needs and achieving market acceptance among patients, physicians and clinicians; our expectations regarding
reimbursement for our approved products from third-party payers; our expectations regarding our relationships with Philips and Siemens, and our ability to achieve compatibility of our systems
with MRI scanners produced by other manufacturers; our ability to attract, develop and maintain relationships with other suppliers, manufacturers, distributors and strategic partners; our
expectations regarding our pipeline of product development, including expanding the clinical application of our products to cover additional indications; our expectations regarding current and
future clinical trials, including the timing and results thereof; our expectations regarding receipt of additional regulatory approvals for our products and future product candidates; our mission and
future growth plans; our ability to attract and retain personnel; our expectations regarding our competitive position for each of our products in the jurisdictions where they are approved; our ability
to raise debt and equity capital to fund future product development, pursue regulatory approvals and commercialize our approved products; and anticipated trends and challenges in our
business and the markets in which we operate.
Forward-looking statements involve known and unknown risks, uncertainties and other factors which may cause the actual results, performance or achievements of the Company to be
materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. The results, performance and achievements of the Company
will be affected by, among other things, such as risks related to our limited operating history and history of net losses; risks related to our ability to commercialize our approved products,
including expanding our sales and marketing capabilities, increasing our manufacturing and distribution capacity, increasing reimbursement coverage for our approved products and achieving
and maintaining market acceptance for our products; risks related to the regulation of our products, including in connection with obtaining regulatory approvals as well as post-marketing
regulation; risks related to our successful completion of clinical trials with respect to our products and future product candidates; risks related to managing growth, including in respect of
obtaining additional funding and establishing and maintaining collaborative partnerships, to achieve our goals; risks related to competition that may impact market acceptance of our products
and limit our growth; risks relating to fluctuating input prices and currency exchange rates; risks related to the reimbursement models in relevant jurisdictions that may not be advantageous; risks
related to reliance on third parties, including our collaborative partners, manufacturers, distributors and suppliers, and increasing the compatibility of our systems with MRI scanners; risks related
to intellectual property, including license rights that are key to our business; and risks related to the loss of key personnel, and such other risks detailed from time to time in the other publicly filed
disclosure documents of the Company which are available at www.sedar.com. The Company’s forward-looking statements are made only as of the date of this presentation and, except as
required by applicable law, Profound disclaims any obligation to update any forward-looking statements, whether as a result of new information, future events or results or otherwise, unless
required by applicable law. There can be no assurance that forward-looking statements will prove to be accurate, as actual results and future events could differ materially from those anticipated
in such statements. Accordingly, and because of the above-noted risks, uncertainties and assumptions, readers should not place undue reliance on forward-looking statements due to the
inherent uncertainty in them.
TULSA-PRO and SONALLEVE are registered trademarks of Profound Medical Corp.
2
Forward-Looking Statements
3
Market and Industry Data
Market data and industry forecasts contained in this presentation have been obtained from industry publications, various publicly available sources and subscription-based reports as well as
from management’s good faith estimates, which are derived from management’s knowledge of the industry and independent sources that management believes to be reliable. Industry
publications, surveys and forecasts generally state that the information contained therein has been obtained from sources believed to be reliable. We have not independently verified any of the
information from third-party sources nor has it ascertained the validity or accuracy of the underlying economic assumptions relied upon therein. We disclaim responsibility or liability in respect of
any third-party sources of market and industry data or information, to the extent permitted by law.
Use of Projections
This presentation contains financial forecasts with respect to our estimated future performance. Our independent auditors have not audited, reviewed, compiled or performed any procedures
with respect to the projections for the purpose of their inclusion in this presentation and, accordingly, neither of them expressed an opinion or provided any other form of assurance with respect
thereto for the purpose of this presentation. These projections should not be relied upon as being necessarily indicative of future results.
In this presentation certain of the above-mentioned projected financial information has been included (in each case, with an indication that the information is an estimate and is subject to the
qualifications presented herein) for purposes of providing comparisons with historical data. The assumptions and estimates underlying the prospective financial information are inherently
uncertain and are subject to a wide variety of significant business, economic and competitive risks and uncertainties that could cause actual results to differ materially from those contained in the
prospective financial information. Accordingly, there can be no assurance that the prospective results are indicative of our future performance or that actual results will not differ materially from
those presented in the prospective financial information. Inclusion of the prospective financial information in this presentation should not be regarded as a representation by any person that the
results contained in the prospective financial information will be achieved.
U.S. FDA Cleared, August 2019
Ablation of Prostate Tissue
“My life
should
not have
to change”
5
Prostate Anatomy
Source: Kirby (1997) An Atlas of Prostatic Diseases, The Encyclopedia of Visual Medicine Series.
6
Current Approaches to Prostate Disease
Active Surveillance
Radical Prostatectomy
Radiation Therapy
Simple
Prostatectomy
Low Risk Intermediate Risk High RiskBenign Salvage / Palliative
Organ Confined Prostate Cancer
• 175,000 new prostate cancer patients diagnosed each year according to the American Cancer Society, 2.9 million US patients living with prostate cancer on active surveillance.
• 300,000 BPH surgeries per year in the US based upon CMS data.10 million US patients living with BPH.
• Radiation failure and palliative patients have limited treatment options.
• Approx 10% of prostate cancer patients undergo other treatments such as HIFU, Laser and Cryo.
1. Real-time MR imaging
• Customized treatment plan
2. Transurethral directional ultrasound for thermal ablation; water cooling of urethra and rectum
• Sweeping ultrasound, continuous rotation (no risk of cold spots between discrete sonications)
• Capable of treating both large and small prostate volumes
• Thermal protection of important anatomy
3. Closed-loop process control software
• Real-time temperature feedback provides for gentle and precise ablation
7
Customizable, Predictable, Incision-Free
TULSA-PRO
prostate
Transurethral applicator
Heating patternIndividually
controlled Transducer elements
bladder
Endorectal cooling device
8
TULSA Flexibility
Whole gland
ablation
Post radiation
failure ablative
therapy
Targeted
ablation
Targeted ablation
of a benign large
prostate
Targeted ablation of a
benign large prostate
with malignant lesion
Customizable, Predictable, Incision-Free
9
Pivotal study of whole-gland ablation in a clinically-significant patient population
TACT: Clinical Trial Design
Study Population• n = 115, 13 clinical sites, 5 countries
• 45 – 80 years old
• Low (33%) & intermediate risk (67%) prostate cancer
Ablation Treatment Plan• Treatment intent was whole-gland ablation with sparing of the urethra
and urinary sphincter
• Recommended by FDA to determine substantial equivalence with
predicate devices and comparison with standard of care
Primary Endpoints (12 months)• Safety: Frequency and severity of adverse events
• Efficacy: PSA reduction ≥ 75% (in > 50% of patients)
Secondary Endpoints (to 5 years)• Prostate volume reduction at 1 year
• Prostate biopsy at 1 year in all patients
• Multi-parametric MRI at 1 year (Central Radiology Lab, Cleveland Clinic)
• Functional Disability: EPIC, IIEF, IPSS
0% 20% 40% 60% 80% 100%
Baseline Patient Prostate Cancer Disease
Clinically significant GG2+ disease
High volume GG1 disease
(≥ 3 cores or ≥ 50% CCL)
Low volume GG1 disease
(Very Low Risk)
10
TACT: Prostate Ablation Efficacy
PSA primary efficacy endpoint resolutely met:
• Primary endpoint of PSA reduction ≥75% was achieved in 110 of 115 (96%)
• Median (IQR) PSA reduction was 95% (91-98%)
• Median PSA nadir was 0.34 (0.12-0.56) ng/ml
Pre-Treatment 12 Month PSA Nadir
N 115 115 115
Median 6.26 0.53 0.34
IQR 4.65 – 7.95 0.28 – 1.25 0.12 – 0.56
Average 6.72 0.93 0.51
T-Test against baseline <0.001 <0.001
Biopsy Outcomes (1-year, 10-core TRUS, High Sampling Density 0.4 cc / core)
• Only 4 of 115 follow-up biopsies are missing, all due to patient refusal
• Among men with pre-treatment intermediate-risk GG2 disease, 54 of 68 (79%) were free of GG2 disease
• Of men with one-year biopsy data, 72 of 111 (65%) had complete histological response and were free of any evidence of cancer
• 41% (16 of 39) of positive biopsies were clinically insignificant (Very Low Risk)
• Multivariate Analysis: Among men with pre-Tx GG2 disease and w/o calcifications at screening, 51 of 60 (85%) were free of GG2 disease
11
TACT: Histological Response
0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100%
12 Months
Baseline
TACT Histological Status (n=115)Clinically significant GG2+ disease
High volume GG1 disease
Insignificant disease (low volume GG1)
No histological evidence of disease
Missing Biopsy
0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100%
Radiation
Clinically significant disease
Insignificant disease (positive w. Tx effect)
No histological evidence of disease
External Beam Radiation Meta-Analysis*
*GCP-10102 available upon request
12
TACT: Prostate Volume Reduction
Prostate volume significantly reduced demonstrating effective prostate ablation• Median perfused prostate volume decreased 91% from 37 cc to 3 cc, on MRI at 1 year (central radiology)
• Prostate ablation confirmed on Contrast Enhanced MRI immediately after TULSA and during follow-up
Follow-up prostate MRI predicts clinically significant disease on biopsy• Multivariate Analysis: Absence of PIRADS ≥ 3 lesion at 1-year post-treatment MRI has 92% Negative Predictive Value for absence of GG2
disease on 1-year biopsy (local radiologists, same as diagnostic PIRADS)
• Ongoing work: Adjusting PIRARDS for post-ablation setting, MRI has 96% Negative Predictive Value for absence of GG2 disease on
1-year biopsy (central radiology)
Immediate PostCE-MRI
PSA 6.0 ng/ml
1 month PostCE-MRI
PSA 0.3 ng/ml
3 months PostCE-MRI
PSA < 0.1 ng/mlPSA < 0.1 ng/ml
0.5 cc
12 months PostT2w MRI
ScreeningT2w MRI
PSA 5.5 ng/ml
58 cc
13
TACT: Erectile Function
Erectile Function, at one year:
• 23% surgeon-assessed moderate erectile dysfunction (CTCAE Grade 2, intervention such as medication indicated)
• 0% any occurrence of severe erectile dysfunction (CTCAE Grade 3, intervention such as medication not helpful)
• 75% (69/92) of previously potent patients maintained erections sufficient for penetration
• Phase I 90% ablation, TACT whole gland ablation
0%
20%
40%
60%
80%
100%
0 2 4 6 8 10 12
IIE
F Q
2 ≥
2, %
Patients
Months
Patients Potent at Baseline (n=92)
TACT
Phase I
0%
20%
40%
60%
80%
100%
0 2 4 6 8 10 12
Months
All Patients (n=110)
75%
85%
14
TACT: Urinary Incontinence
Urinary Incontinence, at one year:
• 2.6% surgeon-assessed moderate urinary incontinence (CTCAE Grade 2, pads indicated)
• 0% any occurrence of severe urinary incontinence (CTCAE Grade 3, operative intervention indicated)
• TACT Urinary Continence (pad use) similar to Observation arm of PIVOT study
0
20
40
60
80
100
0 2 4 6 8 10 12
% P
atients
Months
PIVOT 1
0
20
40
60
80
100
0 2 4 6 8 10 12
% P
atients
Months
TACT
1. Wilt et al, The New England Journal of Medicine, 2017
TULSA, ≤ 1 pad / day
TULSA, no pads
Observation, ≤ 1 pad / day
Observation, no pads
Prostatectomy, ≤ 1 pad / day
Prostatectomy, no pads
Literature Review
Prostatectomy Radiation HIFU
16 – 24% +Margin 1
(Meta-Analysis)
10 – 15% +Margin 2 (RCT)
24% +Margin 3 (ProtecT)
28% Clinically significant 4
20% Insignificant disease 4
(Positive w. treatment effect)
52% Negative 4
59 – 61% Negative 5-6
(Intent to treat)
63% Negative, after 40% having
repeat HIFU and 39% ADT 7
79% 9
(Range: 25 – 100%)1-4
63% 9
(Range: 7 – 85%) 1-5
58% 7
(Range: 44 – 67%) 6-8
15% 9
(Range: 0 – 50%) 1-4
4% 9
(Range: 2 – 15%) 1-5
3% 5
(Range: 3 – 22%) 6-8
9% 11
(Range: 3 – 26%) 1-4
2% 11
(Range: 1 – 9%) 1-5
35% 5
(Range: 9 – 35%) 6-8
15% 9
(Range: 0 – 24%) 1-4
25% 9, 12
(Range: 0 – 40%) 1-5
7% 5
(Range: 1 – 21%) 6-8
15
TACT summary, Literature review of other trials provided for context
Biopsy /
Histology
Erectile
Dysfunctionerections insufficient
for penetration
Urinary
Incontinencemoderate to severe
Urethral
Stricturemoderate to severe
GI Toxicity, moderate to severe
diarrhea, urgency,
incontinence, fistula
TACT Study
TULSA
21% Clinically significant
14% Insignificant disease(GG1, ≤2 cores, < 50% CCL)
65% Negative
23% Grade 2 medication indicated.
No Grade 3 ED
2.6% Grade 2 pads indicated.
No Grade 3 Incontinence
2.6%
No GI Toxicity
1. 1. Tewari et al 2012 (Meta-Analysis)
2. Yaxley et al 2016 (RCT)
3. Hamdy et al 2016 (ProtecT)
4. Radiation Meta-Analysis (publication pending)
5. FDA IDE Study K153023
6. FDA IDE Study DEN150011
7. Crouzet et al, Eur Urol 2014 (1000+ patients, Whole-gland HIFU)
8. Thompson (Chair) et al, AUA prostate cancer clinical guideline update
panel, J Urol 2007
9. Resnick et al, Prostate Cancer Outcomes Study (PCOS), NEJM 2013
10. Potosky et al, Prostate Cancer Outcomes Study (PCOS), J NCI 2004
11. Elliott et al, CaPSURE database, J Urol 2007
12. Budaus et al, Review, Eur Urol 20012
• Subgroup analysis of Phase I patients with baseline IPSS ≥ 12 (n = 9/30)
• No Grade 3 adverse events, erectile function (IIEF) stable from 15±9 to 16±9
• Elterman et al, Prostate Cancer and Prostate Diseases, 2019 (Under Review)
16
BPH Subgroup Analysis of Phase I Study
Characteristics (n=9) Baseline 12 months Change (%)
IPSS 16.1 ± 3.8 6.3 ± 5.0Δ -9.8 ± 7.1
(-58%)
IPSS QoL 2.8 ± 1.1 0.8 ± 1.0Δ -2.0 ± 1.7
(-66%)
Prostate Volume (cc) 54 ± 23 14 ± 5Δ -40 ± 24
(-70%)
Peak flow (Qmax, ml/s) 14.5 ± 4.1 21.9 ± 12.7Δ +7.4 ± 13
(+60%)
Predictable and Targeted Ablation
Bilateral sparing
ablation of cancerous
prostate tissue
Targeted & customized
ablation of diseased
prostate tissue
Ablation of benign tissue
17
18
Clinical Application of TULSA
Low Risk Intermediate Risk High RiskBenign Salvage / Palliative
Organ Confined Prostate Cancer
Large prostate BPH 1
• Preservation of
ejaculatory function
• Combined with
targeted cancer
ablation
• Prophylactic ablation
of suspicious MRI
lesion
Recurrence after radiation 8
• Localized recurrences have
limited options, and morbidity is
high
Palliative locally advanced 9
• Severe urinary symptoms
including BOO with retention
and/or intractable hematuria
Oligometastatic 10
• Benefit to locally treat prostate
• Often radio-recurrent
Customized ablation 2-7
• Targeted ablation (focal)
• Large ablation (wide margins)
• Whole gland ablation (with urethral sparing)
1. Elterman et al, Prostate Cancer and Prostate Diseases, 2019 (Under Review)2. Ramsey et al, The Journal of Urology, 20173. Chin et al, European Urology, 20164. Bonekamp et al, European Radiology, 20185. Eggener et al, The Journal of Urology, 2019 (AUA Abstract)
6. Anttinen et al, International Journal of Hyperthermia, 20197. Anttinen et al, Scandinavian Journal of Urology, 2019 (Under Review)8. Suomi et al, ISTU Barcelona, Spain, 2019 (Conference)9. Sainio et al, ISTU Barcelona, Spain, 2019 (Conference)10. Physician interest
19
Commercial Application of TULSA
Prostatectomy Radiation TULSA
Throughput,
Procedures/Day
2 typically, 3 on a
longer day
Multiple sessions:
5 to 40, 4 - 8 weeks
• 4 in a routine day
• Consistent
treatment times
Patient Recovery WeeksDeterioration over
time
• 2 days
• Minimal need for
pain management
20
TULSA-PRO System Components
Disposable
Applicators
Surgeon Console
Control Room
Energy
System
Robotic Arm,
Computer Hardware
Compatible with MR from leading companies, Philips and Siemens
Capital Equipment One-Time Consumables
21
U.S. Market Entrance Strategy
1. Increasing awareness of TULSA-PRO technology and the TACT clinical data
• TACT clinical data presented at >8 conferences (AUA, EAU, RSNA)
• TULSA-PRO and TACT clinical data presented to >50 institutions
2. Early adopter pipeline developed through interest from clinical presentations
3. Potential delivery channels for TULSA-PRO
• Imaging centers
• Urology practice co-ops who focus on new technologies
• Large opinion leading hospital-based practices
4. Recurring revenue business model
5. ‘Profound Genius Services’ launched to support early adopters
22
Building Our Brand: Low-Cost / High-Impact Patient Awareness Initiatives
Profound Branded Patient Marketing
A. TULSA Patient Website
• EU/APEC site launched
• U.S. site in development
• Global TULSA-PRO site locator
B. Corporate Website enhancement
• Language accessibility
• Blog development with patient-focused material
• TULSA clinical data webpage
C. Video Patient & Physician Testimonials
• Cross platform promotion across
- YouTube channel
- Patient resources
- Social media
Customer Branded Patient Marketing
A. TULSA Patient Marketing
• Patient brochure
• Patient procedure pamphlet
B. TULSA Digital Marketing
• Site branded testimonials
• Digital marketing collateral as required
- Ad campaigns
- Social media collateral
• FDA cleared
• Performed widely by many physicians across United States (warrants new CPT code)
• Frequency consistent with intended clinical use (common conditions have higher volume)
• Consistent with current medical practice (mentioned in guidelines/policies)
• Clinical Efficacy (documented in “top 5” peer-reviewed publications, judged by CPT Panel)
• 1+ reference in a majority US patient population
• 2+ references with no overlapping patients or authors
• 1+ reference with Level of Evidence IIa (review of large long-term cohort studies) or Level I (randomized
controlled trials)
23
Reimbursement: AMA Requirements for Category I CPT Code
SourceL https://www.ama-assn.org/practice-management/cpt/criteria-cpt-category-i-and-category-iii-codes
Why This is a Good Plan
• Unify device indication with coding and TULSA value proposition (1 CPT for multiple prostate diseases)
• Level 1b data in both BPH and Cancer
• Meet CPT & payer requirements (level of evidence, US patients, exclusive authors, exclusive patients)
• Sponsor: TACT 2.0 (n=35), BPH (n=96), Salvage (n=68) = 199 TULSA-PRO Treatments
• Registry: FLEX protocol (and/or SPARED) to get more data at low cost to Profound
• Minimize company-paid procedures, while also providing runway for teaching sites as we motivate them to perform patient pay
Rationale Level N US % Start
1. TACT 2.0 5-year TULSA US Momentum at key teaching sites
Increase US patient %
Re-treat TACT 1.0 patients
2b 115
(+35=150)
48%
(60%)
Started
2. BPH RCT 6-month Anchor study for Level 1 data
Backup plan (next slide)
1b 144 in 2:1
96 TULSA
~100% 2020
3. Salvage 1-year Strong clinical value & entry into guidelines
Need to sponsor or too slow with patient pay
2b 68 ~100% 2020
4. Primary Cancer Meta-Analysis
(Phase I, EU, Registry)
% Ablation vs. Outcomes 2a
5. Single/Small-center Cancer RCT
TULSA vs. Radiation
(Turku, UWO, US?)
Small RCT, 50+ pts, good chance to randomize
Level 1 data in cancer, even if not traditional
Offloads sponsor requirements from Profound
1b 50 minimum 0%
(more)
2020
24
Reimbursement: Clinical Evidence Plan
Publication Package
Oncology, Highly Symptomatic Chronic Diseases
25
Building an Incision- and Radiation-free Ablative Therapeutic Platform
Longer
Term
26
SONALLEVE
CURRENT APPROVALS
• Europe: CE Marked
• China: CFDA Approved
Over 200 publications from leading U.S. &
European clinicians and hospitals
• Uterine Fibroid Treatment
• Bone Metastasis Pain
• Pediatric bone
• Hyperthermia
• Abdominal cancer
27
SONALLEVE: Market Development Strategy
1. U.S. & Western Markets
• Partner with Cologne to continue to develop critical clinical data for cancer and highly symptomatic chronic diseases
• Deploy recurring revenue business model for all new clinical applications
• Enter U.S. market with Humanitarian Device Exemption indication (similar to orphan drug indication for rare diseases)
- Application filed with FDA
- FDA manufacturing site inspection completed successfully
• Potential applications include:
1. Pain management
2. Osteoid Osteoma
3. Pancreatic cancer
4. Hyperthermia
5. Neuro-modulation
2. China
1. Continue working with Philips as distribution partner, in concert with a small Profound direct sales team
2. Marketing for treatment of uterine fibroids
3. Reference site in S. Korea, treating 200 patients/year
28
In Summary
Introducing TULSA-PRO to U.S. market
Business model designed to be capital efficient
• TULSA-PRO: focus on U.S.
• Sonalleve: focus on Asia with larger distribution partner
Future investments:
• Strategically expand U.S.-based sales team as we continue to work with MRI partners, Philips and Siemens
• Clinical trials for TULSA-PRO for reimbursement
• Continued product evolution